Tetraspanins in extracellular vesicle formation and function

被引:1063
作者
Andreu, Zoraida [1 ]
Yanez-Mo, Maria [1 ]
机构
[1] Hosp Santa Cristina, Inst Invest Sanit Princesa, Unidad Invest, Madrid 28009, Spain
来源
FRONTIERS IN IMMUNOLOGY | 2014年 / 5卷
关键词
biogenesis; extracellularvesicles; exosomes; biomarkers; tetraspanin-enriched microdomains; antigen presentation; CELL-DERIVED EXOSOMES; II-PEPTIDE COMPLEXES; T-CELLS; ENRICHED MICRODOMAINS; METASTASIS SUPPRESSOR; TRANSMEMBRANE-4; SUPERFAMILY; ENDOTHELIAL-CELLS; MEMBRANE-VESICLES; LOADED EXOSOMES; DENDRITIC CELLS;
D O I
10.3389/fimmu.2014.00442
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Extracellular vesicles (EVs) represent a novel mechanism of intercellular communication as vehicles for intercellular transfer of functional membrane and cytosolic proteins, lipids, and RNAs. Microvesicles, ectosomes, shedding vesicles, microparticles, and exosomes are the most common terms to refer to the different kinds of EVs based on their origin, composition, size, and density. Exosomes have an endosomal origin and are released by many different cell types, participating in different physiological and/or pathological processes. Depending on their origin, they can alter the fate of recipient cells according to the information transferred. In the last two decades, EVs have become the focus of many studies because of their putative use as non-invasive biomarkers and their potential in bioengineering and clinical applications. In order to exploit this ability of EVs many aspects of their biology should be deciphered. Here, we review the mechanisms involved in EV biogenesis, assembly, recruitment of selected proteins, and genetic material as well as the uptake mechanisms by target cells in an effort to understand EV functions and their utility in clinical applications. In these contexts, the role of proteins from the tetraspanin superfamily, which are among the most abundant membrane proteins of EVs, will be highlighted.
引用
收藏
页数:12
相关论文
共 158 条
[51]   Tetraspanin functions and associated microdomains [J].
Hemler, ME .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (10) :801-811
[52]   Specific tetraspanin functions [J].
Hemler, ME .
JOURNAL OF CELL BIOLOGY, 2001, 155 (07) :1103-1107
[53]   Tetraspanin proteins mediate cellular penetration, invasion, and fusion events and define a novel type of membrane microdomain [J].
Hemler, ME .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2003, 19 :397-422
[54]   The ESCRT Pathway [J].
Henne, William M. ;
Buchkovich, Nicholas J. ;
Emr, Scott D. .
DEVELOPMENTAL CELL, 2011, 21 (01) :77-91
[55]   Annexin A2 recognises a specific region in the 3′-UTR of its cognate messenger RNA [J].
Hollas, Hanne ;
Aukrust, Ingvild ;
Grimmer, Stine ;
Strand, Elin ;
Flatmark, Torgeir ;
Vedeler, Anni .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2006, 1763 (11) :1325-1334
[56]   Direct stimulation of naive T cells by membrane vesicles from antigen-presenting cells: Distinct roles for CD54 and B7 molecules [J].
Hwang, IY ;
Shen, XF ;
Sprent, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) :6670-6675
[57]  
IMAI T, 1995, J IMMUNOL, V155, P1229
[58]  
Karlsson M, 2001, EUR J IMMUNOL, V31, P2892, DOI 10.1002/1521-4141(2001010)31:10<2892::AID-IMMU2892>3.0.CO
[59]  
2-I
[60]   Systemic presence and tumor-growth promoting effect of ovarian carcinoma released exosomes [J].
Keller, Sascha ;
Konig, Anne-Kathleen ;
Marme, Frederik ;
Runz, Steffen ;
Wolterink, Silke ;
Koensgen, Dominique ;
Mustea, Alexander ;
Sehouli, Jalid ;
Altevogt, Peter .
CANCER LETTERS, 2009, 278 (01) :73-81